影响化物产品形成的因素 化物漂白剂和烯反应在气相中的化物产品形成的因素
Callee M Walsh1, Notashia N Baughman1, Jason E Ham1
1Chemical and Biological Monitoring Branch, Health Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, West Virginia 26505, United States.
概括
低化漂白剂释放反应性气体,在室内空气中形成化烯产品. 这项研究确定和量化了这些新型化学物种,揭示了室内空气的重大变化.
科学领域:
- 环境化学环境化学
- 大气化学 大气化学
- 室内空气质量 室内空气质量
背景情况:
- 低化漂白剂是一种常见的家庭产品.
- 使用漂白剂会将低酸 (HOCl) 和 (Cl2) 释放到室内空气中.
- HOCl和Cl2可以与烯等挥发性有机化合物 (VOC) 反应.
研究的目的:
- 为了识别和描述由HOCl/Cl2与烯的气相反应形成的化学物种.
- 量化产品产量,了解反应动力学.
- 研究环境因素对产品形成的影响.
主要方法:
- 气相反应是在特龙室中进行的.
- 用气体染色学和高分辨率质谱学分析了产品.
- 时间采样用于监测反应时间的过程.
主要成果:
- 确定了几种化烯产物,包括烯水素.
- 估计了产品度和产量,超过80%的反应烯.
- 在不同的条件下 (湿度,臭氧,反应剂度) 阐明了反应途径.
结论:
- 漂白剂生成的HOCl/Cl2和利蒙之间的气相反应产生各种化化合物.
- 了解这些反应对于评估漂白剂使用对室内空气质量影响至关重要.
- 环境因素对这些反应产物的形成有很大的影响.
相关概念视频
SN2 Reaction: Kinetics
8.2K
Kinetic Studies and Significance
In a chemical reaction, a relationship exists between the concentration of reactants and the rate at which the reaction proceeds. The study to measure this relationship is known as the kinetics of a chemical reaction. Kinetic studies are used to deduce the rate law of a chemical reaction, which provides information about the species involved during the transition state of the rate-determining step. Thus, kinetic studies help to derive the mechanism of a...
In a chemical reaction, a relationship exists between the concentration of reactants and the rate at which the reaction proceeds. The study to measure this relationship is known as the kinetics of a chemical reaction. Kinetic studies are used to deduce the rate law of a chemical reaction, which provides information about the species involved during the transition state of the rate-determining step. Thus, kinetic studies help to derive the mechanism of a...
8.2K
Reactions at the Benzylic Position: Halogenation
2.4K
Benzylic halogenation takes place under conditions that favor radical reactions such as heat, light, or a free radical initiator like peroxide.
2.4K
Hydrolysis of Chlorobenzene to Phenol: Dow Process
2.6K
Simple aryl halides do not react with nucleophiles under normal conditions. However, the reaction can proceed under drastic conditions involving high temperatures and high pressure to give the substituted products. For example, chlorobenzene is converted to phenol using aqueous sodium hydroxide at 350 °C under high pressure by the Dow process. The reaction follows an elimination-addition mechanism involving a benzyne intermediate. Here, the chloride ion is...
2.6K
Nucleophilic Substitution Reactions
16.0K
Historical perspective
In 1896, the German chemist Paul Walden discovered that he could interconvert pure enantiomeric (+) and (-) malic acids through a series of reactions. This conversion suggested the involvement of optical inversion during the substitution reaction. Further, in 1930, Sir Christopher Ingold described for the first time two different forms of nucleophilic substitution reactions, which are known as SN1 (nucleophilic substitution unimolecular) and SN2 (nucleophilic substitution...
In 1896, the German chemist Paul Walden discovered that he could interconvert pure enantiomeric (+) and (-) malic acids through a series of reactions. This conversion suggested the involvement of optical inversion during the substitution reaction. Further, in 1930, Sir Christopher Ingold described for the first time two different forms of nucleophilic substitution reactions, which are known as SN1 (nucleophilic substitution unimolecular) and SN2 (nucleophilic substitution...
16.0K
Formation of Halohydrin from Alkenes
12.7K
An alkene, such as propene, reacts with bromine in the presence of water to yield a halohydrin. Halohydrins contain a halogen and a hydroxyl group attached to adjacent carbons. When the halogen is bromine, it is called a bromohydrin, while a chlorohydrin has chlorine as the halogen.
12.7K
Electrophilic Aromatic Substitution: Chlorination and Bromination of Benzene
7.7K
Chlorination and bromination are important classes of electrophilic aromatic substitutions, where benzene reacts with chlorine or bromine in the presence of a Lewis acid catalyst to give halogenated substitution products. A Lewis acid such as aluminium chloride or ferric chloride catalyzes the chlorination, and ferric bromide catalyzes the bromination reactions. During the bromination of alkenes, bromine polarizes and becomes electrophilic. However, in the bromination of benzene, the bromine...
7.7K


